Family Wellness Cherry Cough Drops Menthol cough suppressant/Oral Anesthetic recall
FDA recall D-0331-2024 · initiated Jan 19, 2024
Bestco LLC recalled Family Wellness Cherry Cough Drops Menthol cough suppressant/Oral Anesthetic in Jan 2024 — an FDA Class II recall (D-0331-2024) because CGMP Deviations: Potential Glass and Silicone particulates in product.
May cause temporary or medically reversible harm; low probability of serious harm.
Why it was recalled
CGMP Deviations: Potential Glass and Silicone particulates in product
Something got into the product
A physical or chemical contaminant was found — glass or metal fragments, or a solvent that should not be there.
This is a manufacturing or quality failure, not a finding that the medicine is unsafe to take — across every recall we hold, none was issued for that reason. It does not mean the batch was harmless.
Is your product affected? Check the lot number
A recall covers only specific lots. Find the lot number and expiration date on your package and compare them to the affected codes below — if yours is not listed, it was not part of this recall.
Quantity recalled: 46 cases/6 pack each
Details
- Product
- Family Wellness Cherry Cough Drops Menthol cough suppressant/Oral Anesthetic, 80 drops per bag, item number 20001187, Bestco, 288 Mazeppa Road, Mooresville, NC 28115
- Recalling company
- Bestco LLC
- Classification
- Class II
- Status
- Terminated
- Type
- Voluntary: Firm initiated
- Distribution
- Nationwide in the US
- Initiated
- Jan 19, 2024
- FDA report date
- Feb 28, 2024
Frequently asked
- Was Family Wellness Cherry Cough Drops Menthol cough suppressant/Oral Anesthetic recalled?
- Bestco LLC recalled Family Wellness Cherry Cough Drops Menthol cough suppressant/Oral Anesthetic in Jan 2024 — an FDA Class II recall (D-0331-2024) because CGMP Deviations: Potential Glass and Silicone particulates in product. May cause temporary or medically reversible harm; low probability of serious harm.
- Why was Family Wellness Cherry Cough Drops Menthol cough suppressant/Oral Anesthetic recalled?
- Per the FDA enforcement record, the reason for recall D-0331-2024 was: CGMP Deviations: Potential Glass and Silicone particulates in product
- Is a recalled Family Wellness Cherry Cough Drops Menthol cough suppressant/Oral Anesthetic dangerous to take?
- An FDA recall removes specific lots from the market for a defined reason and does not by itself mean the medicine is unsafe for everyone — your specific lot may never have been affected. May cause temporary or medically reversible harm; low probability of serious harm. Check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This reproduces public FDA data and is not medical advice.
- Which lots of Family Wellness Cherry Cough Drops Menthol cough suppressant/Oral Anesthetic are affected?
- Distributed: Nationwide in the US. The recall covers these lots — 100042290, Exp 12/31/2026. Check the lot number and expiration date on your package against this list; if yours is not listed, it was not part of recall D-0331-2024.